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维奈克拉用于不适合强化化疗的老年急性髓系白血病患者:前景、耐药机制与管理策略

英文原题:Venetoclax for elderly patients with acute myeloid leukaemia unfit for intensive chemotherapy: Prospects, resistance mechanisms and management strategies.

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Venetoclax for elderly patients with acute myeloid leukaemia unfit for intensive chemotherapy: Prospects, resistance mechanisms and management strategies.

PubMed 2026/09/01(内容时间) Clin Transl Med Q1 · IF 7.9(JCR 2025)

研究概要

然而,约30%的患者对基于venetoclax的联合方案无应答,且大多数初始应答者最终会复发。

中文摘要

迄今为止,急性髓系白血病(AML)的治疗仍然是血液系统恶性肿瘤中的一大挑战,尤其是在不适合强化化疗的老年患者中。BCL-2抑制剂venetoclax联合azacitidine已显著改善该患者群体的预后和生存。然而,约30%的患者对以venetoclax为基础的联合方案无应答,且大多数初始应答者最终会复发。因此,venetoclax耐药已成为限制其长期临床获益的关键瓶颈。深入理解其潜在耐药机制并开发克服耐药的新策略,是改善老年AML患者生存结局的核心。venetoclax的耐药机制复杂且涉及多方面,包括TP53突变、FLT3-ITD和NRAS/KRAS突变等遗传驱动因素,以及抗凋亡蛋白(如MCL-1、BCL-xL)上调、代谢重编程和细胞分化状态改变。针对这些因素,新兴治疗策略正迅速向精准化和联合方案方向发展,包括与靶向药物(如IDH2抑制剂、FLT3抑制剂)联合、MCL-1抑制剂、优化当前给药方案(如DEC3-VEN),以及开发新型治疗模式(如抗体药物偶联物、CAR-T细胞疗法)。本叙述性综述聚焦老年AML的疾病特征,总结venetoclax的临床疗效,批判性审视venetoclax耐药的多方面机制,并讨论当前及新兴的克服耐药的治疗策略。目的是为临床实践提供信息并指导未来的转化研究。关键要点:本综述阐明了venetoclax当前的作用机制、治疗效果和局限性,重点关注其在不适合强化治疗的老年AML患者这一特定人群中的使用和联合方案,以及克服耐药的策略,并为应对venetoclax耐药提供未来展望。

展开英文摘要原文

To date, the treatment of acute myeloid leukaemia (AML) remains a major challenge in hematologic malignancies, particularly among elderly patients who are unfit for intensive chemotherapy. Venetoclax, a BCL-2 inhibitor, in combination with azacitidine, has significantly improved the prognosis and survival of this patient population. However, approximately 30% of patients do not respond to venetoclax-based combination regimens, and most initial responders eventually experience relapse. Therefore, resistance to venetoclax has become a critical bottleneck limiting its long-term clinical benefits. A thorough understanding of the underlying resistance mechanisms and the development of novel strategies to overcome resistance are central to improving survival outcomes in elderly AML patients. The resistance mechanisms of venetoclax are complex and multifaceted, including genetic drivers such as TP53 mutations, FLT3-ITD, and NRAS/KRAS mutations, as well as the upregulation of anti-apoptotic proteins (e.g., MCL-1, BCL-xL), metabolic reprogramming, and altered cellular differentiation states. In response to these factors, emerging therapeutic strategies are rapidly evolving toward precision-based and combination approaches, including combinations with targeted agents (e.g., IDH2 inhibitors, FLT3 inhibitors), MCL-1 inhibitors, optimization of current dosing regimens (e.g., DEC3-VEN), and the development of novel modalities (e.g., antibody-drug conjugates, CAR-T cell therapy). Focusing on the disease characteristics of elderly AML, this narrative review summarizes the clinical efficacy of venetoclax, critically examines the multifaceted mechanisms of venetoclax resistance, and discusses current and emerging therapeutic strategies to overcome this resistance. The goal is to inform clinical practice and guide future translational research. KEY POINTS: This review elucidates the current mechanism of action, therapeutic effects, and limitations of venetoclax, focusing on its use and combination regimens in the specific patient population of elderly individuals with AML who are not suitable for intensive therapy, as well as strategies to overcome resistance, and provides future perspectives for addressing venetoclax resistance.

论文信息

作者
Zhang J、Liu J、Zhao M、Zhang X、Liu L、Li M、Cao C、Zhang R
第一作者单位
First Central Hospital of Tianjin Medical University, Tianjin Medical University, Tianjin, China.China
通讯作者单位
Department of Hematology, Tianjin First Central Hospital, Tianjin Thrombosis and Hemostasis Institute, Tianjin, China.China
文献类型
综述
期刊
Clinical and translational medicine2026 Sep
原文标识
PubMed 42661469 · DOI 10.1002/ctm2.70797